Aria Corao
Aria Corao
Profesor ingles
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TítuloCitado porAño
Analysis of the Micro‐RNA‐133 and PITX3 genes in Parkinson's disease
L de Mena, E Coto, LF Cardo, M Díaz, M Blázquez, R Ribacoba, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153 …, 2010
712010
Mitochondrial DNA haplogroups in Spanish patients with hypertrophic cardiomyopathy
MG Castro, C Huerta, JR Reguero, MI Soto, E Doménech, V Alvarez, ...
International journal of cardiology 112 (2), 202-206, 2006
702006
FGF20 rs12720208 SNP and microRNA-433 variation: no association with Parkinson's disease in Spanish patients
L de Mena, LF Cardo, E Coto, A Miar, M Díaz, AI Corao, B Alonso, ...
Neuroscience letters 479 (1), 22-25, 2010
552010
SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V
E Sánchez‐Ferrero, E Coto, C Beetz, J Gamez, AI Corao, M Diaz, ...
Clinical genetics 83 (3), 257-262, 2013
542013
Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia
V Álvarez, E Sánchez-Ferrero, C Beetz, M Díaz, B Alonso, AI Corao, ...
BMC neurology 10 (1), 89, 2010
492010
Non-invasive genetic study of the endangered Cantabrian brown bear (Ursus arctos)
T Pérez, F Vázquez, J Naves, A Fernández, A Corao, J Albornoz, ...
Conservation genetics 10 (2), 291-301, 2009
442009
A Search for SNCA 3′ UTR Variants Identified SNP rs356165 as a Determinant of Disease Risk and Onset Age in Parkinson’s Disease
LF Cardo, E Coto, L de Mena, R Ribacoba, O Lorenzo-Betancor, P Pastor, ...
Journal of Molecular Neuroscience 47 (3), 425-430, 2012
412012
Mitochondrial transcription factor A (TFAM) gene variation and risk of late-onset Alzheimer's disease
V Alvarez, AI Corao, C Alonso-Montes, E Sanchez-Ferrero, L De Mena, ...
Journal of Alzheimer's disease 13 (3), 275-280, 2008
392008
Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H
M Palacín, V Alvarez, M Martín, M Díaz, AI Corao, B Alonso, ...
Mitochondrion 11 (1), 176-181, 2011
342011
Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's disease
V Alvarez, AI Corao, E Sánchez-Ferrero, L De Mena, C Alonso-Montes, ...
Neuroscience Letters 432 (1), 79-82, 2008
342008
Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier
E Coto, M Palacín, M Martín, MG Castro, JR Reguero, C García, ...
Journal of translational medicine 8 (1), 64, 2010
252010
Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy
E Coto, J Gómez, B Alonso, AI Corao, M Díaz, M Menéndez, C Martínez, ...
Neurogenetics 12 (4), 345-346, 2011
242011
Apolipoprotein ε4 allele is associated with psoriasis severity
P Coto-Segura, E Coto, V Alvarez, B Morales, J Soto-Sánchez, AI Corao, ...
Archives of dermatological research 302 (2), 145-149, 2010
232010
Evidence for improved connectivity between Cantabrian brown bear subpopulations
T Pérez, J Naves, JF Vázquez, J Seijas, A Corao, J Albornoz, ...
Ursus 21 (1), 104-109, 2010
212010
Resequencing of the IL12B gene in psoriasis patients with the rs6887695/rs3212227 risk genotypes
N Eiris, J Santos-Juanes, P Coto-Segura, J Gómez, V Alvarez, B Morales, ...
Cytokine 60 (1), 27-29, 2012
172012
Functional polymorphisms in the CYP3A4, CYP3A5, and CYP21A2 genes in the risk for hypertension in pregnancy
E Coto, B Tavira, R Marín, F Ortega, C López-Larrea, M Ruiz-Ortega, ...
Biochemical and biophysical research communications 397 (3), 576-579, 2010
152010
Myocyte enhancing factor-2A in Alzheimer's disease: genetic analysis and association with MEF2A-polymorphisms
P González, V Álvarez, M Menéndez, CH Lahoz, C Martínez, AI Corao, ...
Neuroscience letters 411 (1), 47-51, 2007
152007
Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease
A Miar, V Álvarez, AI Corao, B Alonso, M Díaz, M Menéndez, C Martínez, ...
Brain research 1383, 252-256, 2011
122011
Resequencing the whole MYH7 gene (including the intronic, promoter, and 3′ UTR sequences) in hypertrophic cardiomyopathy
E Coto, JR Reguero, M Palacín, J Gómez, B Alonso, S Iglesias, M Martín, ...
The Journal of Molecular Diagnostics 14 (5), 518-524, 2012
112012
Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia
E Sánchez-Ferrero, E Coto, AI Corao, M Díaz, J Gámez, J Esteban, ...
Journal of neurology 259 (2), 246-250, 2012
92012
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
Artículos 1–20